Department of Gynecological Oncology, National Women's Health at Auckland City Hospital, Auckland, New Zealand; Department of Obstetrics and Gynecology, University of Auckland, New Zealand.
Department of Obstetrics and Gynecology, University of Auckland, New Zealand.
Gynecol Oncol. 2020 May;157(2):450-455. doi: 10.1016/j.ygyno.2020.01.029. Epub 2020 Feb 7.
To investigate the incidence and survival of Vulvar Squamous Cell Carcinoma (VSCC) by etiology over a 27 year period.
Retrospective case-note and pathology slide review of 390 consecutive VSCC, treated at a Centralized Cancer Centre covering half New Zealand's population, 1990-2016. Incidence was calculated in 5-6 year cohorts and correlated with precursor of the VSCC, age and stage.
Age-standardized incidence of all VSCC did not change significantly, however age standardized incidence of HPV-dependent VSCC increased significantly, from 0.55/100,000 (95% CI 0.38-0.72) in 1991-2000 to 0.83/100,000 (95% CI 0.68-0.97) in 2001-2016, with a significant decrease in the incidence of HPV-independent VSCC, from 0.76/100,000 (95% CI 0.58-0.95) to 0.54/100,000 (95%CI 0.43-0.65). HPV-dependent VSCC in women ≥50 years increased significantly from 0.75/100,000 (95% CI 0.45-1.17) to 1.43/100,000 (95% CI 1.14-1.77), with no significant change seen in younger women. HPV-independent VSCC in women ≥50 years has decreased significantly from 2.53/100,000 (95% CI 1.95-3.23) to 1.62/100,000 (95% CI 1.31-1.98) with no change in younger women. The proportion of HPV-dependent VSCC has increased from 25% to 50%. Age standardized death rate from VSCC has not changed significantly from 0.22/100,000 (95% CI 0.10-0.34) in 2001-5 to 0.27/100,000 (95% CI 0.15-0.40) in 2011-16. Five year survival for HPV-dependent VSCC was 93% and 68% for HPV-independent VSCC (p < .0001).
HPV-dependent VSCC incidence has increased significantly and now accounts for half of VSCC, with a significant rise in women over 50. HPV-dependent and independent VSCC have different prognoses and should be registered and investigated separately.
通过 27 年的时间,调查外阴鳞癌(VSCC)按病因的发病率和生存率。
对在一个覆盖新西兰一半人口的集中癌症中心治疗的 390 例连续 VSCC 的病历记录和病理切片进行回顾性病例分析,时间范围为 1990 年至 2016 年。按 5-6 年的队列计算发病率,并与 VSCC 的前体、年龄和分期相关联。
所有 VSCC 的年龄标准化发病率没有显著变化,然而,HPV 依赖性 VSCC 的年龄标准化发病率显著增加,从 1991-2000 年的 0.55/100,000(95%CI 0.38-0.72)增加到 2001-2016 年的 0.83/100,000(95%CI 0.68-0.97),HPV 非依赖性 VSCC 的发病率显著下降,从 0.76/100,000(95%CI 0.58-0.95)降至 0.54/100,000(95%CI 0.43-0.65)。≥50 岁的女性中 HPV 依赖性 VSCC 的发病率显著增加,从 0.75/100,000(95%CI 0.45-1.17)增加到 1.43/100,000(95%CI 1.14-1.77),年轻女性中没有显著变化。≥50 岁的女性中 HPV 非依赖性 VSCC 显著下降,从 2.53/100,000(95%CI 1.95-3.23)降至 1.62/100,000(95%CI 1.31-1.98),年轻女性中没有变化。HPV 依赖性 VSCC 的比例从 25%增加到 50%。VSCC 的年龄标准化死亡率从 2001-5 年的 0.22/100,000(95%CI 0.10-0.34)到 2011-16 年的 0.27/100,000(95%CI 0.15-0.40)没有显著变化。HPV 依赖性 VSCC 的 5 年生存率为 93%,HPV 非依赖性 VSCC 为 68%(p<.0001)。
HPV 依赖性 VSCC 的发病率显著增加,现已占 VSCC 的一半,50 岁以上女性的发病率显著上升。HPV 依赖性和非依赖性 VSCC 具有不同的预后,应分别进行登记和研究。